Service Hématologie Greffe, Hôpital Saint-Louis, Université Paris Cité, Paris, France.
Université Paris Est Créteil, INSERM U955 Equipe Transfusion et Maladies du Globule Rouge, IMRB, Créteil, France.
Bone Marrow Transplant. 2024 Sep;59(9):1232-1238. doi: 10.1038/s41409-024-02316-0. Epub 2024 May 25.
In the case of donor/recipient rhesus (Rh)-incompatibility after allogeneic hematopoietic stem cell transplantation (alloHSCT), the transfusion policy in France is to transfuse red blood cells (RBC) in the donor's Rh phenotype from the day of transplantation, leading to a risk of allo-immunization, either of donor or recipient origin. In this single-center retrospective study, the incidence of donor/recipient Rh incompatibility was 7.1% over an 8-year period including 1012 alloHSCT. Six of 58 evaluable patients (10.3%) developed alloantibodies to RBC antigens within one year of alloHSCT. None of these allo-immunizations were directed against the donor-mismatched Rh antigens and none could have been prevented by the transfusion of recipient and donor Rh-compatible RBC units. None of these allo-immunizations led to immune-mediated hemolytic anemia. We observed a statistically significant higher incidence of chronic GVHD among patients with anti-RBC allo-immunization. In the context of donor/recipient Rh incompatibility, the transfusion of packed RBC units in the donor's Rh phenotype from the day of alloHSCT is feasible and not associated with a high risk of allo-immunization. The generalization of this strategy could be discussed even when donor and recipient Rh phenotypes could be respected, to allow the preservation of units of infrequent phenotypes for other indications.
在异基因造血干细胞移植(alloHSCT)后供体/受者发生恒河猴(Rh)不相容的情况下,法国的输血策略是从移植日起输注供体 Rh 表型的红细胞(RBC),导致供体或受体来源的同种免疫风险。在这项为期 8 年的单中心回顾性研究中,包括 1012 例 alloHSCT 在内,有 7.1%的患者发生供体/受者 Rh 不相容。在 alloHSCT 后 1 年内,58 例可评估患者中有 6 例(10.3%)发生了针对 RBC 抗原的同种抗体。这些同种免疫反应均不是针对供体不相容的 Rh 抗原,且无法通过输注受者和供者 Rh 相容的 RBC 单位来预防。这些同种免疫反应均未导致免疫介导的溶血性贫血。我们观察到,发生抗 RBC 同种免疫的患者慢性移植物抗宿主病的发生率显著更高。在供体/受者 Rh 不相容的情况下,从 alloHSCT 日起输注供体 Rh 表型的浓缩 RBC 单位是可行的,且不会导致同种免疫反应的高风险。即使可以尊重供体和受体的 Rh 表型,也可以讨论这种策略的推广,以便为其他适应证保留稀有表型的单位。